HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 391408Erstellt: 25. Oktober 2026
Triphenylphosphine → 3-(Bromomethyl)-5-(trifluoromethyl)benzonitrile
https://huagongshe.com/reaction/391408
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Edukt | N-bromobutanimide | HCID 67184 | — |
| Edukt | 3-(Hydroxymethyl)-5-(trifluoromethyl)benzonitrile | HCID 11701221 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 3-(Bromomethyl)-5-(trifluoromethyl)benzonitrile | HCID 11601369 | — |
Reaktionsschritte
3-(Hydroxymethyl)-5-(trifluoromethyl)benzonitrile (0.33 mg, 1.64 mmol) and triphenylphosphine (0.86 g, 3.28 mmol) were combined in methylene chloride (6 mL) and cooled to 0° C. N-Bromosuccinimide (0.61 mg, 3.43 mmol) was introduced in portions and the reaction allowed to warm to room temperature. After 16 h, the reaction mixture was diluted with methylene chloride, washed with concentrated sodium bicarbonate (2×), brine (2×), dried over sodium sulfate, and concentrated. Column chromatography on silica gel (20% ethyl acetate/hexanes) gave 0.36 g (83%). 1H-NMR (CDCl3, 500 MHz) δ 7.97 (s, 2H), 7.84 (s, 1H), 4.50 (s, 2H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08383821B2 |
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| Quelldatensatz | uspto-grants-2013_02 |
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| ORD ID | ord-7e23b24fbf744967ae3683bf41d8c9a8 |
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| Quellennotiz | uspto-grants-2013_02 |
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